NDC 65862-230

Lamotrigine 200 mg tablet

On the label: Aurobindo Pharma Limited.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Aurobindo Pharma LimitedMedchal, IndiaMakes it and tests it Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action

Product details

Generic drug
Lamotrigine: every company that makes it
Form
tablet, oral
Strength
200 mg
Approval
ANDA ANDA078956
On the market since
Jan 27, 2009
Package NDCs
65862-230-01 65862-230-10 65862-230-60 65862-230-78 65862-230-99
Official label
DailyMed (National Library of Medicine), updated May 25, 2026

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